Application of an Intelligent Pain Monitoring System during Painful Procedures in Preterm Infants across Different Gestational Age Groups

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2600129654

Enrollment

Unknown

Registered

2026-08-07

Start date

2026-08-08

Completion date

Unknown

Last updated

2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain assessment

Interventions

Newborn group:None

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.preterm infants with a gestational age of less than 37 weeks; 2.preterm infants requiring painful procedures for therapeutic purposes; 3.Those undergoing continuous electrocardiographic monitoring; 4.Those whose parents or legal guardians provided informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Limited body position (fractures, etc.); 2. Those with severe conditions requiring emergency treatment; 3. Those who have pain reactions due to diseases or other factors.

Design outcomes

Primary

Measure	Time frame
Intensity of pain;Evaluate the accuracy, stability, applicability and safety of the intelligent pain monitoring system.;	—

Countries

China

Contacts

Public ContactHuang Yi

Affiliated Hospital of Zunyi Medical University

245794952@qq.com+86 852 28609562

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026